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Biblical Wanderings: Mark 2 and 11

Then a paralytic was brought to him, carried by four. Since they were unable to get to him through the crowd, they uncovered the roof above him, made an opening, and lowered the paralytic on his mat. And Jesus saw their faith, and said to the paralytic, “Son, your sins are forgiven.” (Mark 2:3-5)

And they were walking back in the morning, and saw the fig tree withered from the roots. Peter remembered and said, “Look, Rabbi! The fig tree you cursed has withered.” “Have faith in God,” Jesus said to them. “Truly I tell you that if anyone says to this mountain, ‘Be lifted up and thrown into the sea’, and has no separation from this desire in his heart, but believes that it will happen, it will be done for him. Therefore I tell you, as much as you ask in prayer, believe that you have received, and it will be yours. And when you stand to pray, if you hold anything against anyone, forgive, so that your father in heaven will forgive your trespasses as well.” (Mark 11:20-25)

“There is nothing wrong with you.” Love wrote this in my journal last week, after a half an hour of waiting, pen to paper. Instantly I felt great relief. He didn’t mean that there was nothing wrong with my body - that would have been a cruel message, after spending the last few days in bed, feeling histamine waves soar through my body, limbs buzzing madly, stomach white-hot as it tried to digest my latest meal. What his message reassured me of was that there was nothing wrong with me. It wasn’t my fault I was sick. There wasn’t something I was doing wrong that had cursed my life to be what it was. It simply was what it was, and it had nothing to do with me - the real me. 

In my experience, it’s almost impossible to be sick without also feeling wrong. Sickness places a barrier between us and the usual comforts of society. People say they hope you’ll feel better soon, and you imagine a deadline being placed in their mind, their increasing impatience and demand on you if you don’t feel better soon. “Do you know what caused this relapse?” translates in my mind to: what did you do this time? “Have you tried x type of doctor/treatment yet?” translates to: why haven’t you fixed yourself yet? People offer their kindnesses and sympathies in whatever ways they know how, and none of it sinks in, and you feel awful for it. I’m not just sick, I’m a bad person - wouldn’t a better person be able to receive this comfort? Shouldn’t it make a difference? 

It isn’t surprising to me that Jesus forgives the sick man’s sins before he heals his body. He is a healer of the soul first, and in comparison with bodily pain, that guilty, anxious, unending torment is the far worse suffering. 

But that’s at the start of Mark, when we have a healthy Jesus, healing the sick. By the time we get to the story of the fig tree, it’s Jesus that is in distress. He knows he’s facing his imminent end, knows that this trip to Jerusalem will be his last. He is staring death in the face, and yet must continue getting on with the basic necessities of life. This is the paradox that every sick person finds themselves in: figuring out how to live while being exiled from life. I can’t help but read his words here as more of a reminder to himself than a lesson to his disciples. Why did he curse the fig tree? Why does anyone curse anything? It’s being in that cursed state, that state of exile, where we feel a million miles away from everyone and everything, and are expected to traverse that distance for every interaction and task we’re faced with. Divorced from love and grace, the lines of empathy and connection that bond us with life - many of which we don’t see even in good health - vanish into the haze of alienation.

There’s nothing harder than believing in love and life in the face of this world as we encounter it. Those times of easy comfort, when we feel safe in our bodies and our surroundings, seem like little oases stretched out among a vast and desolate landscape. We encounter some intuitive understanding of what it’s like to be loved, and then that intuition is stripped away, and we’re asked to keep believing it as we walk through the fire.

Maybe that’s why Jesus reminds his disciples, or himself, or his father, to forgive: because he knows now how hard it is. Nobody knows how hard it is to walk this life until they start walking it. That is the power of the story of Jesus - that he was willing to walk through it, to encounter every emotion and situation and every darkness that a human faces. That is the thrill of our own lives, that we might be willing to walk through and live through a reality that has more pain and more complexity and more beauty than our minds and bodies are built to comprehend. No human can walk that path without falling, because we’re not built for it. But we are built to harbor and bring forth these immense powers of belief and empathy, to dig a well in the desert and find water.

For thirty years of my life I was terrified about getting sick. The idea that the thing I was currently doing might lead to long-term health complications down the road, or that the pain I was feeling might be cancer, kept me in a state of constant distraction. Then I actually got sick, and discovered that in 30 years I had never been well. I had lived with this anxiety, assuming it was an innate part of myself; I had listened to the stories it told. Once I was sick, I found out that these stories were…incomplete. After all, how could my anxiety have the whole picture, tell an accurate story, if I’d never actually lived through a sickness? So I did start living through sickness, and discovered that there was life in sickness. I encountered love while being sick. I learned and grew stronger within myself while I was sick. My body got better, than worse again, then hovered, then changed. Simple narratives about success and failure, a healthy life or a descent towards death, did not apply. All I could say, all I can say, is that I’m living inside a less-than-perfect body.

What is this thing called life that flows through our veins? Surely we understand it to be more than a beating heart and breathing lungs. When we speak of life we speak of happiness, hope, the ability to see morning sunlight and call it beautiful, the spirit that drives us to engage with the larger world. When these things fade out of our life, what is left? Can it be called life? Yet the paralyzed man didn’t need happiness and hope; all he needed was patience and forbearance with his friends, who did have hope, as they tried increasingly reckless ways to bring him back into the fullness of life. This less-than-perfect body is a workshop, where everything is uncertain and experimental, where necessity is the mother of invention, where the gritty realities of mortal life are revealed in all their painful glory. Job screams, “I am nothing but skin and bones; I have escaped only by the skin of my teeth,” and three thousand years later, I’m listening as I lie in bed and he’s killing me softly with his song, telling my whole life with his words. Those who are reduced to skin and bones sing the deepest, most beautiful elegies. We learn the truth about life when we decide to walk through it, and we carry that truth to everyone we meet.

Biblical Wanderings: Mark 2 and 11

Comments

All I have ever known is sickness. All I have ever known is pushing myself through that sickness. There is beauty in the suffering, when your bones break they never heal quite the same. But I wouldn’t be me without all the struggles I have endured to get here. I have become stronger, and built an endurance and appreciation for the heartache. As a means of survival, you learn to alchemize that pain into something more digestible. Once you start breathing easier, and your mind begins to clear - you realize that it was worth all the suffering. Love is a trial by fire. I have just about burnt myself to the ground, but I keep moving because that love and pain is all I know. It gets easier with time, the human body is an incredible thing. One day I am sick and covered in rug burns, the next I am moving about regardless. I’ll always be alright, because I have love in my heart.

Sam Bradley

I also have OCD, and my story is similar to yours. I was also terrified of being sick, to the point where I was staying up crying and shaking when someone in my family was sick. If it was a stomach virus I’d be so anxious that I’d start feeling sick anyways, which would make matters worse. I had a few months in elementary school where I felt sick almost all the time, starting when a friend of mine came home from camp with Noral virus and threw up after being in a long car ride with me. I would refuse to admit if I was sick if I was, because it felt like weakness, moral and physical. I associated sickness with a sort of inhuman state, where being around others could infect them. I was also obsessed with the idea that the mind could control the body. I was so afraid of losing control that I would refuse laughing gas at the dentist. But as I grew out of my fear of sickness, I began a trial of an adhd med, which gave me sexual side effects that resulted in 13 year old me discovering that I was attracted to the same sex. I was horrified that I couldn’t control my sexuality; trying to repress and manipulate it failed and I ended up suicidal, now devoid of sickness of the body but still contagious and inhuman, a true moral failing, a sickness of the mind that couldn’t even conform to mother nature’s rules. I am also a writer (not poetry though) and it feels like the only way to express my experience. I don’t think I will ever reach an equilibrium with my body and mind, but I am learning to make the mind less important. Hope it goes well with you.

Alex

Howdy

duke

Marlboro spotted 👀

1 buck danger

i regret taking so long to listen and read up on this series. i hope someone is still able to read what i have to say, but there's worth in just saying it any way. i've always been so scared of physical pain and physical ailments. it's probably a big part of living with ocd: when i feel compassion for others in pain and my empathy takes over, the sheer fear of truly going through that pain is almost paralysing. there has been countless times where i'd have to calm myself down from thinking i was able to bring myself to illness or any other sort of physical pain through my thoughts alone. i've always been obssessed with the idea that my brain could somehow impact my life or my body. i've been carrying this belief for so long that, when i got off depression meds and lost some weight for it, i thought i got skinny through the sheer power of my mind - i've always been bigger than my sister and that had bothered me my entire life. it was proof: my mind could change me, if i want it to enough. it was proof and that was all i wanted, so i held onto it: developing an eating disorder was the obvious next step to ensure the power i was so sure i had over my body. and then came true sickness: feeling cold, bloating constantly; sometimes my feet would be hurt from constant exercise. i was always angry and defensive, couldn't work or hang out w friends or have sex w my partner or think about social issues. nothing really mattered because my body needed constant vigilance. i remember the health obssession was ever-present and it literally made me sick. my thought process & my inner world have always had this divine aspect to them. i've always lived inside my own head: i have gone through so many paths & circumstances & love stories & tragedies inside my brain that sometimes life just doesn't seem real enough to me. i've been writing poetry for as long as i can remember - possibly ever since becoming literate, but at 26 i've never published anything. i'm a writer - in my head, at least. i've published a book in my fantasy world, and it's so hard to understand that that's not enough. it's not enough. i need to live it. life is strange like that. i live here (in my body) and also here (in my head) and the line between it all has always been striking to me. it's there, clear as day; i know where my body ends and my mind begins, and i choose the latter constantly. i neglect the body because i can't control it - i've tried and all it did was made me want to annihilate it. my mind is easier, however it's not real: there's no connecting inside it, there's no true satisfaction & fullfilment. but ah is it safe. and it's mine. i've been making a real effort to walk the walk, though. it truly takes strength and purpose to live in the real world. it takes belief and understanding and choice; responsability is something i'd always run away from, so this is good & new. my inner world will always be rich and beautiful (and so completely mine), but i know what it takes to become. i must do it. sorry for the rambling. this has been great. goodbye.

Raíssa Leão

it always ends up okay, sometimes we forget that. thank you for the support <3

duke

it’s going to be ok 🫀 thank u for sharing

marlowe green

I found myself boomeranging back and forth between the big picture of major life struggle and then to the day to day. I thought of my peril filled journey through addiction into recovery 25 years ago. And also how the expectation that I should feel and be better today is a sometimes crippling lie. I am alive and making my way. Sometimes drawing comfort, sometimes giving it. Sometimes seeing beauty. Sometimes not even looking for it. I appreciate you Will. May you be the most well you can be in whatever way is possible today. ❤️

Jim Kennedy

There were so many thoughts and feelings expressed here that I’ve felt my whole life and had not really sat to process before. I grew up around illness, my grandma died after a long illness (I still remember visiting her at the hospital every week as a kid), the aunt I’m named after died from cancer right before I was born, my dad was sick and disabled my entire childhood and I have always lived in a constant state of thinking I’m seriously ill too, when I wasn’t. Most of my childhood anxieties (lol and now too) revolve around health, my body and death. Now , I am starting to experience some health concerns that affect my life and while I’m trying to figure things out with doctors, life does have to keep going :’) Chronic body pain, blood pressure and migraines are a few of the things that affect me most day to day not just physically but mentally. After talking to the doctor about my health and getting not so great news … we decided that I needed to move more and chose something kinda crazy to achieve that goal 😅 I like what you said about living life through sickness and living life in a less than perfect body because it became most relevant to me Friday night! I decided to take up ballet , at 27 and being a little on the chubby side, I decided to fulfil my childhood dream of learning ballet (I danced as a little kid , ballet and Mexican folk dancing but it was too expensive to continue). Had my first class yesterday despite a headache , and my body hurting and I being tired from my endless week , I went anyway (I paid for classes I have to go) and it was beautiful and … really hard 🥺 I was terrible at it lol But it’s not about being perfect , it’s about finding joy and having a healthier relationship with my body . I’m not trying to become a professional ballerina , and I’ll need to accept that my less than perfect body is not always gonna perform to Royal Academy standards. But this class was so kind and so fun and I’m glad I could try something new! And I was told I kept up well for my first class in 20 years!! I’ve been thinking about this BW all week bc I’ve been feeling sick and burnt out and just crawling to our break time bc I don’t have enough days I can just take off (either for rest or doctors appointments) and it validated some things I’ve felt my whole life and validates my current experience. My girlfriend is a brain cancer survivor (we take headaches seriously around here!) and I appreciate her perspective a lot too of once you have been sick and have to live with sickness (or the aftermath of an illness) it becomes another part of your life, but not your entire life. We can still dance in our own ways and find love and joy despite our bodies not being perfect. It’s also useless to compare ourselves to others bc we all have our own journeys at our own paces! It’s a weird experience standing at a wall to wall mirror with other people and it’s hard not to compare to others - oh her toes are more pointed and her turn out is better and they’re more coordinated than me and would I look like that if I lost a few lbs ahhh … But I try to remember that other people have similar thoughts and are probably looking at me the same way I look at them … This was a lot sorry, but you and your words have been on my mind all week. Hope you’re staying safe, warm and happy 💕 it’s finally springtime!!

Carmen✨

This post helped soothe my soul in ways I didn’t think were possible. I feel like I’ve been living my life like the narrator from Notes From The Underground: convinced he’s sick and will die soon, yet unsure of what it is that’s killing him. What you said about fearing getting sick your whole life and having the reality not match what your anxiety told you it would be like when you were ill was, maybe, selfishly, something I needed to hear. My anxieties and fears are not prophecies - I believe you when you say there is life in sickness, and I feel more ready than ever to embrace that sickness and try to get better. I love you, this band, and this community. I hope we all can gather the strength to walk through life and realize that what we think we know might not always be correct. It's okay to be wrong. I'm mostly saying this for myself, I guess, and as a thank you, if it can be called one. Thank you.

Jake

Thank you for this. I hope you know the value your words have for people. I'm in my late 20s and am just beginning to take stock of, and try to come to some kind of terms with, the enormous impact illness has had on my life and the lives of those I love. My mum died when I was 16 after a fairly long illness, and in recent years I have become carer for my dad, who has multiple sclerosis. I also have issues with my body which are too complex to go into here, but which, as you described, make me feel far removed from society and the ordinary joys and comforts of life. The things you've expressed here about the peculiar difficulties, as well as the hard won solaces of illness, put into words things I've never fully managed to articulate to myself. Most important of all to me is the sense of hope which you manage to convey. It's a hope that I project deep into the past for my mum, that I wish for for my dad, for myself, for you, and for everyone who struggles in this way.

lewis

yeah this one hits close! ive been suffering from chronic nausea since i was a teenager and growing up through it, and trying to live despite it. its difficult to sit down and acknowledge that i have an illness i have to live with, for whatever reason. i think it is partly because living while sick; going out, maintaining relationships, getting a job, etc. are all put on hold when placed in the context of short term illnesses; every time i have a cold, or another infection, the part of me that yearns for it to pass quickly is stuck arguing with the other part of me that cries, "but you'll still be sick afterwards." accepting that the illness is a part of you is something im not sure anyone can ever do fully (but hey maybe im still just rebelling against it) but its a struggle for me because it feels like admitting defeat. if i cry and thrash and scream against it maybe it'll go away quicker, but when i hurt my body the only thing that gets hurt is me. the paralytic man needing patience -- i think people tend not to understand fully how debilitating chronic illnesses can be and getting someone to understand what you feel is done by pleading with them and hoping they believe you. if that patience, that acknowledgement of what your body can/cannot do isn't given by other people its incredibly hard to give it to yourself. people can tell you that you shouldn't feel guilty but that guilt is so overwhelming; since I was a kid i've had in my head over and over again the demand of, "why cant you just do things like a normal person?" and the desire to pretend your body works as normal means you cant work with what it really is, and it burns you out and makes you hate it, despite it being a part of you. its a constant battle between, 'I have to live with it,' and, 'I have to live despite it,' and, 'I cant live with it.' i dont have any grand conclusions about how to find happiness in the face of it because im still figuring that out -- ive only recently started to move away from constantly denying im ill. i hope everyone else here who is ill finds that happiness. its a lonely, difficult, life-long journey that no one asks for, its not your fault, and there is a way to live with it/despite it, i still havent figured out which one is best :-)

virtualdotshelf

I had long covid while I was a teenager in high school, and for a long time I felt that the so-called “best years of my life” were being wasted rotting in bed. It was as if the outside world was a mere screen projection, and all I could do was sit back and watch the shadows flicker on the cave wall. No one tells you that the most straining symptoms of long term illness is boredom.

gumby

I’ve been sick. at least that’s how i’ve explained it to my little sister. my doctors have been telling me that it’s as if my depression was a physical ailment, the way i couldn’t move, couldn’t leave bed, couldn’t eat. I hated that the people I love have had to watch me fade away. They’ve watched me crumple into a shell of the person I once was. I don’t like telling her that her older brother is sick. That she doesn’t know exactly what’s wrong with me, and she begs me to get better soon. I’m not sure how to get better. I don’t know if I’ve ever been better. I feel like I’m taking too long, that I’m overdramatic, I should be over this by now. I’d like to think I’m getting better, but I just don’t know. I really liked this weeks, it made me cry a bit, but in a good way. It’s going to be okay. Eventually. Probably. That’s all for this week I guess

duke

sorry guys i’m getting to it, very very busy last couple weeks i seem to have no time for anything anymore

duke

Tom

marlowe green

listening to this, I started to cry. illness is often so isolating, especially as a young individual. i’ve been learning to navigate my own chronic illnesses and disabilities for over a decade and it just does not get easier. what you said about finding what makes life worth living rings so true. this past summer I was diagnosed with glaucoma and told that I was going blind, as a visual artist, this was my last straw. finding meaning in life when everything that gave it meaning is stripped away is a truly humbling and nauseating experience. there is solace in knowing and hearing that we aren’t alone in illness. thank you for this, and sending love <3

everette

Where’s it at tommy

Holiday

i love your writing; the words you choose and the way you combine them into beautiful and poetic sentences giving them this power of touching other's souls in particular ways. you were in my thoughts this week, too. i hoped you were alright, as far as possible. i, too, feel wrong. i've been struggling with my health - mental and physical - for a while now. most days i can't function properly and even though there are people who care about me, their words slip through me like sand would slip through our fingers. "you are going to get better" when? how much time do i have? what do i need to do in order to achieve this? it's taking too long and sometimes i'm afraid people will end up giving up on me because of that, even if they say they won't. accepting comfort can be as hard as getting out of bed. am i disappointing people because i'm taking too long to get better? each day i hold up to little things that make me remember i'm alive, despite the pain that comes from this act. my cats' purring, someone saying something funny during classes, a deep conversation with one of my professors before i take the bus... we always try to attribute meaning to life despite the circumstances. but there are times the pain is too intense, and i feel like nothing will ever compensate it. like last week: i've been struggling with an intense abdominal pain for a few months now, i still don't know what's causing it because i don't have money to see a doctor (even though i could use universal health care, i am afraid of doctors because i have a dark past of transphobia coming from them). i woke up in a cold sweat because of this pain and it was so intense i started crying out of frustration. i knew i would have to cancel at least half of the plans i had made because of it. i have an idea of what's happening: poor nutrition. because of financial difficulty and chaotic routine, my diet got really bad... unfortunately. truth is even though i feel bad when people say it to me, i want things to get better. so i lay down (when possible) and pray for it to happen. for this moment to come. and sometimes i feel like i believe it is coming. i am learning, little by little, to forgive myself for feeling pain. i am learning to live through it. i know our pains are different, but i sympathize with yours. much love to you ❤️. i wish i could express myself better in english though... hope i'm on the right path despite the language limitations.

damian

you were in my thoughts on monday. i hoped, unfairly, that you weren’t in pain, wherever you were. before i started testosterone, i had chronic menstrual pain. once, a cyst on one of my ovaries ruptured, and i was so bewildered from the pain that all the memories of my life shrunk away, and my whole consciousness had honed to simple breathing. when the menstrual pain would be particularly bad, i would feel like an animal; there was nothing left that was human about me, and i was reduced to the most basic functions. i relate to the frustration of loved ones saying, essentially, “i hope you’re not in pain.” and yet… “this pain is a part of me,” i would think in frustration. “are you afraid of this part of me? do you wish i was different, that i didn’t have this dark, cruel, inconvenient thing? what if i cannot rid myself of it, what if it stays forever? will you hate a part of me forever?” and yet i wish every day that other people’s pain was gone. i don’t want people to suffer. i don’t want my friends who live with chronic illness to suffer. do i truly accept that their pain may be lifelong? again and again i pray, or promise (as much as either is worth) to have unconditional love for all parts of them. i still live with chronic conditions - thankfully, no chronic pain anymore - and i paradoxically still feel the frustration at well-intentioned people who want me to ‘get better’, even though i still have passing hopes like this for others. i think it’s just the limits of our language manifesting compassion. instead of “i hope you aren’t in pain”, something more useful might be “what can i do for your pain?” i would go to the ends of the earth for a loved one who was in pain; i *know* the panic and vulnerability of severe, unending, complex pain, and would do anything, anything to alleviate it in others, to offer whatever small comfort or encouragement or solidarity. i struggle with some of the ideas within the healing miracles of Jesus. will i remain autistic in heaven? to what end are painful symptoms faults to be healed, cured, fixed? to what end are disability and pain ‘bad’? there are aspects of the experience of pain that i find beautiful, and have enhanced my compassion for the pain of others. is pain a human experience, not a divine one? on the contrary, i have never felt closer to God than when i am curled in the foetal position, panting like an animal, brain addled by the stabbing of a white-hot blade. a flaming sword like the one Jophiel wields in Eden. thank you for this wandering; it’s really relatable and offers a kind and thoughtful perspective. much much solidarity to you.

Luka Buchanan

Really enjoyed listening to this one. as someone who’s never been able to write well, your words are so beautiful. Sending over warm thoughts. I hope spring makes everyone a bit brighter with all of the new plant life coming back

Enoch

i'll be back after classes, as always! :)

damian

rhis is beautifully written oh my gosh

alex

i’ll type out my paragraph soon

duke


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